Guest guest Posted September 27, 2001 Report Share Posted September 27, 2001 Welcome to the group Krissy!!! I have three girls as well!! How old are your girls mine are 10, 6, 5 and we hope to have that little reversal boy very soon. I hope you find all you are looking for here, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 27, 2001 Report Share Posted September 27, 2001 hi krissy, and welcome, you are more than welcome to go with me and jana oct22nd, if insterested e mail me at rosebudd98@..., you will find a wonderful group of girls here, most helpful, write back soon, love judy l Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 27, 2001 Report Share Posted September 27, 2001 Hi, Krissy, where in So Cal. are you? I grew up there and my parents still live there (Villa Park). I went to Cal Start Fullerton for my under grad. Welcome to the group. I'm still going through lots of changes and am not ready to schedule yet. I need to get settled and start my job before I can think about surgery and all that entails, as well as all the personal issues I'm sorting through. But the ladies have been very welcoming and warm in the couple of days I've been with the group, and I'm sure you'll find a buddy! Good luck to you...Syndie > I am new to the group and I would like to introduce myself. My name > is Kris but I go my Krissy. I have 3 daughters and a very devouted > boyfriend of 12 years he is also the father and step-father to my > girls, I had my tubes tied in Aug 94 and that was the worst mistake > of my life it seem like a part of me have died well since the > beginning of this month I have been trying to research all I can on > have the TR done and I am getting a lot of information and advise > from other women who have or going through what I am going through > right now. I live in Southern Ca and I would like to have a reversal > buddy if there is anyone out there please let me know. > Krissy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 9, 2005 Report Share Posted October 9, 2005 Hi Kent, We are all looking for a cure but you will not find it from drugs. Allot of us are on natural treatment. I am using Ambrotose it will make your immune system work better so your body can make you well. I have had MS for 25 years and had given up when I heard about Ambrotose from a friend who had cancer and the Dr's wanted her to take Chemo after surgery, she refused and took Ambrotose instead she is now cancer free. I will send some info to you privately if you are interested. I probably didn't explain it well. but the info i can send you will explain it better. Let me know if you are interested. We must kill this MonSter. Kathy --- KENT WAKEFIELD wrote: > Hello group: > > I would like to ask the group for information that > may be off topic. I would like to know if anyone in > the group has tried xin, Or Tysabri before it > was pulled off the market. > > I realize this may not be the right group to ask > this question but I also know we're all here looking > for the answers to fight multiple sclerosis. > > Thank you take care, Kent > > > [Non-text portions of this message have been > removed] > > __________________________________ Start your day with Yahoo! - Make it your home page! http://www.yahoo.com/r/hs Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 10, 2005 Report Share Posted October 10, 2005 Dear Elize, I believe you have the right idea about multiple sclerosis. It is said that everything happens for a reason. According to Edgar Cayce, multiple sclerosis is, as a rule, meant to be a lesson in soul growth--a spiritual learning experience, if you will--like a refiner's fire purifing a hunk of gold by burning out its impurities. With best wishes, Dudley Delany http://profiles.yahoo.com/dudley_delany Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 10, 2005 Report Share Posted October 10, 2005 > I would like to ask the group for information that may be off topic. I would like to know if anyone in the group has tried xin, Or Tysabri before it was pulled off the market. > AFAIK xin is in clinical trials. From what I've read, I'm *very* excited by its possibilities, and I would be fascinated by a first-hand report from someone in the trials. -Dave Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 10, 2005 Report Share Posted October 10, 2005 I have certainly learned a ton from my illness, but I must say I NEVER accepted it, never invited it to stay, never embraced it in any way. Learned from it, yes, but everything in life is a learning experience. I don't feel we are " Given " illnesses to learn lessons, we get them for many reasons and the learning, and growing that comes from it is a choice we can make,or not. I know some people who have not learned anything from their illness but to become negative and depressed. Everyday that I was sick I was in a battle to get well, for me the " monstor " analogy was very appropriate. -- RE: HI Hi everyone This is Elize from South Africa again. I am still on the long exciting road to recovery and am still positive most days and having been very focused on nutrition and supplements and am now turning more to exercise and spiritual development and growth. My comment is on something that Kathy said. I am saying this with the utmost respect as I am trying really hard at the moment to be positive and make people feel good about themselves but I take exception to people calling MS the monster and that we must kill it. I really and truly believe and have done so every since I was diagnosed that this is a challenge. Everyone gets challenges in their lives and this is ours and we must take MS by the hand and walk with it till the very end. We are here to learn lessons and sometimes we are given obstacles to help us to learn these lessons if we cannot learn them any other way. I used to be a huge go getter living in a fast pased town and I used to wonder why everyone was so slow . . . that is how energetic and fast I was. I have now had to slow down and smell the roses and have discovered how good they smell. I would never have had the chance otherwise. I have by no means finished with my healing however I believe that I am heading in the right direction. Kathy, I hope that you do not take offence to what I said as I always enjoy your posts and find them to be informative and interesting to read. Warm regards Elize Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 10, 2005 Report Share Posted October 10, 2005 Elize, I am sorry that you don't see this disease as a MonSter but after living with this for half of my life I can't think of a more appropriate word. Yes I have chosen to look at things in my life I would change but I could and would have done that anyway without this MonSter. I understand that I wouldn't have met some wonderful people who have helped over the years but I might have met other wonderful people had I been well. I have become a burden to everyone who loves me and brought them worry and sorrow even though I try my hardest not to. I try to bring joy to all who are around me but I can see how they worry about me. I hate what this disease has done to me and all the Dr.'s I have seen but I do know now that Dr.s don't know or care how to make this disease better. I understand what you are saying but how do you know that you wouldn't have discovered those things anyway? Somethings are not to be known. God Bless, Kathy --- " Kindscher (Charter) " wrote: > I have certainly learned a ton from my illness, but > I must say I NEVER > accepted it, never > invited it to stay, never embraced it in any way. > Learned from it, yes, but > everything in > life is a learning experience. I don't feel we are > " Given " illnesses to > learn lessons, we get > them for many reasons and the learning, and growing > that comes from it is a > choice we can > make,or not. I know some people who have not > learned anything from their > illness but to > become negative and depressed. Everyday that I was > sick I was in a battle to > get well, > for me the " monstor " analogy was very appropriate. > > > -- RE: HI > > Hi everyone > > This is Elize from South Africa again. I am still on > the long exciting road > to recovery and am still positive most days and > having been very focused on > nutrition and supplements and am now turning more to > exercise and spiritual > development and growth. > > My comment is on something that Kathy said. I am > saying this with the utmost > respect as I am trying really hard at the moment to > be positive and make > people feel good about themselves but I take > exception to people calling MS > the monster and that we must kill it. I really and > truly believe and have > done so every since I was diagnosed that this is a > challenge. Everyone gets > challenges in their lives and this is ours and we > must take MS by the hand > and walk with it till the very end. We are here to > learn lessons and > sometimes we are given obstacles to help us to learn > these lessons if we > cannot learn them any other way. I used to be a huge > go getter living in a > fast pased town and I used to wonder why everyone > was so slow . . . that is > how energetic and fast I was. I have now had to slow > down and smell the > roses and have discovered how good they smell. I > would never have had the > chance otherwise. I have by no means finished with > my healing however I > believe that I am heading in the right direction. > > Kathy, I hope that you do not take offence to what I > said as I always enjoy > your posts and find them to be informative and > interesting to read. > > Warm regards > Elize > > [Non-text portions of this message have been > removed] > > __________________________________ Yahoo! Music Unlimited Access over 1 million songs. Try it free. http://music.yahoo.com/unlimited/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 10, 2005 Report Share Posted October 10, 2005 Hi Kathy, You bring lots of joy to me, but you are right, I do worry about you. When you are feeling good then I rejoice!! We need more days when you feel good and less bad ones. Keep fighting, you can't lose if you don't give up!!! Blessings, -- RE: HI Elize, I am sorry that you don't see this disease as a MonSter but after living with this for half of my life I can't think of a more appropriate word. Yes I have chosen to look at things in my life I would change but I could and would have done that anyway without this MonSter. I understand that I wouldn't have met some wonderful people who have helped over the years but I might have met other wonderful people had I been well. I have become a burden to everyone who loves me and brought them worry and sorrow even though I try my hardest not to. I try to bring joy to all who are around me but I can see how they worry about me. I hate what this disease has done to me and all the Dr.'s I have seen but I do know now that Dr.s don't know or care how to make this disease better. I understand what you are saying but how do you know that you wouldn't have discovered those things anyway? Somethings are not to be known. God Bless, Kathy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 10, 2005 Report Share Posted October 10, 2005 Hi , Thanks for your concern. Today is a good day so lets keep this going I started the classic Ambrotose on Fri.and not taking so much only about 1 and 1/2 tsp a day. We'll see how that goes. God Bless,Kathy --- " Kindscher (Charter) " wrote: > Hi Kathy, > > You bring lots of joy to me, but you are right, I do > worry about you. When > you are feeling good then I rejoice!! We need more > days when you feel good > and less bad ones. Keep fighting, you can't lose if > you don't give up!!! > Blessings, > > -- RE: HI > > Elize, > I am sorry that you don't see this disease as a > MonSter but after living with this for half of my > life > I can't think of a more appropriate word. Yes I > have > chosen to look at things in my life I would change > but > I could and would have done that anyway without this > MonSter. I understand that I wouldn't have met some > wonderful people who have helped over the years but > I > might have met other wonderful people had I been > well. > I have become a burden to everyone who loves me and > brought them worry and sorrow even though I try my > hardest not to. I try to bring joy to all who are > around me but I can see how they worry about me. > I hate what this disease has done to me and all the > Dr.'s I have seen but I do know now that Dr.s don't > know or care how to make this disease better. > I understand what you are saying but how do you know > that you wouldn't have discovered those things > anyway? > Somethings are not to be known. > God Bless, Kathy > > [Non-text portions of this message have been > removed] > > __________________________________ Yahoo! Mail - PC Magazine Editors' Choice 2005 http://mail.yahoo.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 11, 2005 Report Share Posted October 11, 2005 Thanks! It continues to sound great. There must be a potential downside... (right?) -Dave > dave go to www.ihavems.com to read tims story with tovaxin trials. > > AFAIK xin is in clinical trials. From what I've read, I'm *very* > > excited by its possibilities, and I would be fascinated by a first-hand > > report from someone in the trials. > > > > -Dave > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 12, 2005 Report Share Posted October 12, 2005 Kent, One of the fellows that discovered Interferon back in the 1950's, spent 40 years to develop a natural alternative to Interferon Drugs. Here is a link for more information and links to the clinicals that have been done on this herbal product that gives our bodies the ability to produce our own natural interferon. http://www.shaklee.net/millin_health_for_you/prodNuFeronHome HAVE A GREAT DAY! Ivan > Hello group: > > I would like to ask the group for information that may be off topic. I would like to know if anyone in the group has tried xin, Or Tysabri before it was pulled off the market. > > I realize this may not be the right group to ask this question but I also know we're all here looking for the answers to fight multiple sclerosis. > > Thank you take care, Kent Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 14, 2005 Report Share Posted October 14, 2005 Re xin, here are 2 websites from Tim Wesner, a person with MS who is in the xin trial, describing his results (remember, your results may vary). He has two small websites that show a timeline of events. The first one is: http://www.IHaveMS.com It starts with the first injection and goes for 18 months. The websites are little 10-page boilerplate sites, so the timeline continues on a second website: http://www.TimsWellness.com from June 2004 to the present. > I would like to ask the group for information that may be off topic. > I would like to know if anyone in the group has tried xin, Or > Tysabri before it was pulled off the market. > > > > AFAIK xin is in clinical trials. From what I've read, I'm *very* > excited by its possibilities, and I would be fascinated by a first- hand > report from someone in the trials. > > -Dave > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 21, 2012 Report Share Posted April 21, 2012 wow this is intense you should give it a look http://www.canews15.net/biz/?news=0862135 ~*Advertisement Quote Link to comment Share on other sites More sharing options...
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